Our Professional Staff Provides Smart and Efficient Solutions
We are scientific and regulatory professionals who work closely with our clients to manage risk and drive development and product registration projects forward as quickly and efficiently as possible.
Leadership
Administration
Scientific & Regulatory Consultants

Fernanda Alvarez
Associate
Nonclinical Safety and Development
Nonclinical Safety and Development

Melanie Bell, MS, RAC-Drugs
Principal Consultant
CMC Regulatory Affairs
CMC Regulatory Affairs

Melanie Butler-Gauthier, MS
Senior Consultant
Nonclinical Safety & Development
Nonclinical Safety & Development

Aimee Cousoulis, MS, PMP
Director
CMC & Quality
CMC & Quality

Bettina Donato, DABT
Senior Principal Consultant
Nonclinical Safety & Development
Nonclinical Safety & Development

Jessica Douglas
Consultant
CMC Regulatory Affairs
CMC Regulatory Affairs

Cynthia Fink, MPH
Advisor
Clinical Development & Regulatory Affairs
Clinical Development & Regulatory Affairs

Mary Fisher
Associate Principal Consultant
CMC & Quality
CMC & Quality

Madeline Ganton
Consultant
Regulatory Operations
Regulatory Operations

Kimberly Hoefling, MS
Principal Consultant
Clinical Development & Regulatory Affairs
Clinical Development & Regulatory Affairs

Jennifer Jacobson, MS
Senior Principal Consultant
Clinical Development & Regulatory Affairs
Clinical Development & Regulatory Affairs

Abigail Kisling, MPH
Consultant
Regulatory Operations
Regulatory Operations

Jeffrey Klein, PhD, DABT
Advisor
Nonclinical Safety & Development
Nonclinical Safety & Development

Daniel Krietlow, MA
Associate Principal Consultant
Nonclinical Safety & Development
Nonclinical Safety & Development

Nicole Lay, MS, DABT
Director
Nonclinical Safety & Development
Nonclinical Safety & Development

Jessica Lvov
Associate
CMC Regulatory Affairs
CMC Regulatory Affairs

Dipali MacAllister, PharmD, RPh, RAC-US
Senior Principal Consultant
Clinical Development & Regulatory Affairs
Clinical Development & Regulatory Affairs

Rogelio Martinez Jr, MS
Consultant
Nonclinical Safety & Development
Nonclinical Safety & Development

Dana Minnick, PhD, DABT, RAC-US
Senior Advisor
Nonclinical Safety & Development
Nonclinical Safety & Development

Tara Morgen
Consultant
CMC & Quality
CMC & Quality

Kara Moy
Consultant
CMC & Quality
CMC & Quality

Brian Mulhern, MS, DABT
Senior Principal Consultant
Nonclinical Safety & Development
Nonclinical Safety & Development

Heather Palmer
Associate Director
CMC Regulatory Affairs
CMC Regulatory Affairs

Cameron Pierce
Consultant
Clinical Development and Regulatory Affairs
Clinical Development and Regulatory Affairs

Sara Price, MA
Senior Consultant
Nonclinical Safety & Development
Nonclinical Safety & Development

Jeff Pudlo, PhD
Advisor
CMC & Quality
CMC & Quality

Rajan Ramaswami, PhD
Advisor
CMC & Quality
CMC & Quality

Isabella Rossi
Senior Consultant
CMC & Quality
CMC & Quality

Danielle Ruiz, MS, RAC-US
Associate Principal Consultant
Clinical Development & Regulatory Affairs
Clinical Development & Regulatory Affairs

Beth Silverstein, MS, RAC-US
Senior Scientific Advisor
Clinical Development & Regulatory Affairs
Clinical Development & Regulatory Affairs

Sarah Smith, MS
Associate Director
Regulatory Operations
Regulatory Operations

Christopher Snyder, MS
Manager
CMC Regulatory Affairs
CMC Regulatory Affairs

Nathanael Stocke, PhD
Principal Consultant
CMC & Quality
CMC & Quality

Vivian Vue
Consultant
CMC Regulatory Affairs
CMC Regulatory Affairs

Emily Wagner, PMP
Consultant
CMC Regulatory Affairs
CMC Regulatory Affairs

Stacie Wehling, MSCR, RAC-US
Associate Director
Clinical Development & Regulatory Affairs
Clinical Development & Regulatory Affairs

Cara Weyker, MBA
Senior Advisor
CMC & Quality
CMC & Quality

Kristy White, MS, PMP, CMCCP
Senior Principal Consultant
CMC Regulatory Affairs
CMC Regulatory Affairs

Coua Xiong-Vang, PharmD, MHA
Senior Consultant
Clinical Development & Regulatory Affairs
Clinical Development & Regulatory Affairs

Sharon Young, PhD
Principal Consultant
CMC & Quality
CMC & Quality